Hematology

Safety

HEM-SA

Safety in haematology is mostly about blood — uncapping it, spinning it, spilling it and shipping it. This domain covers the barriers you wear at the bench, the hygiene that keeps contamination from travelling, the rules for moving specimens between sites, and what a technologist does when something in the department is plainly not safe. The items below work through decisions that come up on an ordinary shift. Safety is one of the eight competency areas assessed in the Hematology Fields-of-Practice examination set by CAMLPR.

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Choosing barriers that match the task in front of you

Barrier protection is selected for the job at hand, not worn as a fixed uniform. Gloves and a closed, fluid-resistant laboratory coat are the baseline for anything involving blood; face and eye protection are added whenever a tube is uncapped by hand, a syringe is decanted, or a specimen is mixed hard enough to throw droplets. Gloves come off the moment they are torn or soiled, and always before touching clean surfaces such as keyboards, telephones and door handles. Doffing order matters — the most contaminated item is removed first, and hands are cleaned afterwards.

A technologist must remove the caps from twenty EDTA tubes by hand before setting up manual reticulocyte preparations at an open bench. Gloves and a fluid-resistant laboratory coat are already worn. What additional protection does this task call for?

Partway through loading a rack onto the analyser, a technologist notices a smear of blood on the outer cuff of one glove. What is the correct immediate response?

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Hand hygiene and keeping contamination at the bench

Hygiene is what stops contamination travelling from the bench to your face, your phone and the corridor outside. Hands are cleaned after gloves come off, before leaving the technical area, before eating and after any contact with blood. Alcohol-based rub is fast and effective on hands that look clean, but it does not lift organic soil, so visibly contaminated hands need soap and running water. Food, drink, cosmetics and contact lens handling stay out of the work area, long hair is tied back away from open specimens, and personal items are kept off the bench surface.

After dealing with a specimen bag that had leaked in transit, a technologist finds a visible smudge of dried blood on the back of one hand. Which hand hygiene method is required before work resumes?

A technologist has just finished a run of manual differentials and has removed a pair of intact gloves in order to take a telephone call at the clerical desk. What must happen first?

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Classifying and packing specimens that leave the site

Specimens moving between sites are dangerous goods, and the person who packs them carries part of the responsibility for the shipment. Most diagnostic blood samples travel as UN 3373, Biological Substance, Category B, inside a three-layer system: a leakproof primary tube, a leakproof secondary container holding enough absorbent to take up everything inside it, and a rigid outer box bearing the diamond UN 3373 mark and the proper shipping name. Requisitions ride outside the secondary container. Anyone who classifies, packs, marks or signs for a shipment needs current transport training on file under Canada's dangerous goods rules.

An EDTA specimen is being couriered to a referral laboratory in another city for haemoglobin electrophoresis. The requisition records no highly hazardous pathogen and the patient is an outpatient with a family history of thalassaemia. How should the shipment be classified and marked?

A technologist is assembling triple packaging for a Category B courier run containing four tubes of whole blood. What determines whether the absorbent material inside the package is adequate?

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Specimens from patients under precautions, and aerosol control

Precautions posted on a ward describe how the patient is cared for; they do not change how tightly the tube is wrapped. In the laboratory every specimen is already handled as though it were infectious, so a sample from a patient under contact or droplet precautions is analysed the same way any other is. What genuinely alters risk is aerosol generation: sealed centrifuge buckets are opened only after the rotor has stopped and, where indicated, inside a cabinet; nothing is expelled forcefully from a syringe; spills are disinfected promptly. A bag showing visible leakage is dealt with before the tube inside is opened.

A CBC specimen reaches the haematology bench from a ward patient nursed under contact precautions for a resistant organism. How should the specimen be handled?

At the end of a spin, a technologist lifts a sealed centrifuge bucket and sees broken glass and free blood inside it. What is the safest first action?

HEM-SA-14

Naming hazards and pushing them into the reporting system

Safety only works when problems get said out loud. A technologist is expected to notice the frayed power cord, the unmarked squeeze bottle, the guard interlock that no longer stops a moving probe, the sharps pail filled past its line — and to act rather than quietly work around it. An immediate hazard is made safe or taken out of service, and the concern then goes to the supervisor and into the written reporting system. Near misses are recorded as seriously as injuries, because they are the cheapest warning a laboratory ever receives.

A technologist finds that the guard interlock on an automated haematology analyser no longer halts the sampling probe when the guard is raised. What is the appropriate response?

A working dilution of a haematology stain has been decanted into a plain squeeze bottle and left at the staining bench with nothing written on it. Which statement about labelling that bottle is correct?

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